Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test47 genes linked to Weak cry
Changes in these genes cause rare conditions in which Weak cry is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| AK2adenylate kinase 2 | Always | In 1 condition |
| ATRXATRX chromatin remodeler | Always | In 1 condition |
| CHRNDcholinergic receptor nicotinic delta subunit | Always | In 1 condition |
| DSTdystonin | Always | In 2 conditions |
| EXOSC9exosome component 9 | Always | In 1 condition |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Always | In 1 condition |
| IFT56intraflagellar transport 56 | Always | In 1 condition |
| KDM6Alysine demethylase 6A | Always | In 1 condition |
| KMT2Dlysine methyltransferase 2D | Always | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Always | In 1 condition |
| NDUFS8NADH:ubiquinone oxidoreductase core subunit S8 | Always | In 1 condition |
| NIPBLNIPBL cohesin loading factor | Always | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Always | In 1 condition |
| PEX19peroxisomal biogenesis factor 19 | Always | In 1 condition |
| RAPSNreceptor associated protein of the synapse | Always | In 2 conditions |
| UBA1ubiquitin like modifier activating enzyme 1 | Always | In 1 condition |
| LAMA2laminin subunit alpha 2 | Very often (80–99%) | In 1 condition |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Very often (80–99%) | In 1 condition |
| ASPAaspartoacylase | Often (30–79%) | In 1 condition |
| COL13A1collagen type XIII alpha 1 chain | Often (30–79%) | In 1 condition |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Often (30–79%) | In 2 conditions |
| FKTNfukutin | Often (30–79%) | In 1 condition |
| FTOFTO alpha-ketoglutarate dependent dioxygenase | Often (30–79%) | In 1 condition |
| LAMB2laminin subunit beta 2 | Often (30–79%) | In 1 condition |
| LYRM4LYR motif containing 4 | Often (30–79%) | In 1 condition |
| MAGEL2MAGE family member L2 | Often (30–79%) | In 2 conditions |
| OPA1OPA1 mitochondrial dynamin like GTPase | Often (30–79%) | In 1 condition |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Often (30–79%) | In 1 condition |
| RYR1ryanodine receptor 1 | Often (30–79%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Often (30–79%) | In 2 conditions |
| SIM1SIM bHLH transcription factor 1 | Often (30–79%) | In 1 condition |
| VARS1valyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| VPS13Bvacuolar protein sorting 13 homolog B | Often (30–79%) | In 1 condition |
| ASAH1N-acylsphingosine amidohydrolase 1 | Sometimes (5–29%) | In 1 condition |
| SYT2synaptotagmin 2 | Sometimes (5–29%) | In 1 condition |
| TRIP4thyroid hormone receptor interactor 4 | Sometimes (5–29%) | In 1 condition |
| CHATcholine O-acetyltransferase | Not recorded | In 1 condition |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Not recorded | In 1 condition |
| CHRNEcholinergic receptor nicotinic epsilon subunit | Not recorded | In 2 conditions |
| COQ9coenzyme Q9 | Not recorded | In 1 condition |
Show 7 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| CRYABcrystallin alpha B | Not recorded | In 1 condition |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Not recorded | In 1 condition |
| GGPS1geranylgeranyl diphosphate synthase 1 | Not recorded | In 1 condition |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Not recorded | In 1 condition |
| LAMA3laminin subunit alpha 3 | Not recorded | In 1 condition |
| MUSKmuscle associated receptor tyrosine kinase | Not recorded | In 1 condition |
| TPM3tropomyosin 3 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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